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Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsNeurogeneticsCraniosynostosis GeneticsGenetic DisordersNeurogenetic DisordersRare Disease GeneticsRare Disease GenomicsSyndromic Congenital DisordersSyndromic Etiology
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Noggin, Cartilage Morphogenesis, and Joint Formation in the Mammalian Skeleton
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A human chondrodysplasia due to a mutation in a TGF-β superfamily member
J. Terrig Thomas, Keming Lin, Maithily Nandedkar et al. · Nature Genetics · 1996 · 417 citations · Full text